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人类 DNA 随时间的推移比病毒双链 DNA 降解得更快:使用跨越 85 年的病理学存档样本分析 HPV16。

Human DNA decays faster with time than viral dsDNA: an analysis on HPV16 using pathology archive samples spanning 85 years.

机构信息

Infections and Cancer Laboratory, Cancer Epidemiology Research Program, Catalan Institute of Oncology (ICO), Granvia de L'Hospitalet 199-203, 08908, L'Hospitalet de Llobregat, Spain.

Infections and Cancer Unit, Cancer Epidemiology Research Program, Catalan Institute of Oncology (ICO), Barcelona, Spain.

出版信息

Virol J. 2021 Mar 29;18(1):65. doi: 10.1186/s12985-021-01529-9.

Abstract

BACKGROUND

Quality of the nucleic acids extracted from Formalin Fixed Paraffin Embedded (FFPE) samples largely depends on pre-analytic, fixation and storage conditions. We assessed the differential sensitivity of viral and human double stranded DNA (dsDNA) to degradation with storage time.

METHODS

We randomly selected forty-four HPV16-positive invasive cervical cancer (ICC) FFPE samples collected between 1930 and 1935 and between 2000 and 2004. We evaluated through qPCR the amplification within the same sample of two targets of the HPV16 L1 gene (69 bp, 134 bp) compared with two targets of the human tubulin-β gene (65 bp, 149 bp).

RESULTS

Both viral and human, short and long targets were amplified from all samples stored for 15 years. In samples archived for 85 years, we observed a significant decrease in the ability to amplify longer targets and this difference was larger in human than in viral DNA: longer fragments were nine times (CI 95% 2.6-35.2) less likely to be recovered from human DNA compared with 1.6 times (CI 95% 1.1-2.2) for viral DNA.

CONCLUSIONS

We conclude that human and viral DNA show a differential decay kinetics in FFPE samples. The faster degradation of human DNA should be considered when assessing viral DNA prevalence in long stored samples, as HPV DNA detection remains a key biomarker of viral-associated transformation.

摘要

背景

从福尔马林固定石蜡包埋(FFPE)样本中提取的核酸质量在很大程度上取决于分析前、固定和储存条件。我们评估了储存时间对病毒和人类双链 DNA(dsDNA)降解的差异敏感性。

方法

我们随机选择了 44 例 1930 年至 1935 年和 2000 年至 2004 年期间采集的 HPV16 阳性浸润性宫颈癌(ICC)FFPE 样本。我们通过 qPCR 评估了同一 HPV16 L1 基因(69 bp,134 bp)两个靶标与人类微管蛋白-β基因(65 bp,149 bp)两个靶标在相同样本中的扩增情况。

结果

所有储存 15 年的样本均能扩增出病毒和人类的短靶标和长靶标。在储存 85 年的样本中,我们观察到较长靶标扩增能力显著下降,且人类 DNA 的差异大于病毒 DNA:与病毒 DNA 相比(95%CI 1.1-2.2),人类 DNA 中较长片段的恢复可能性低 9 倍(95%CI 2.6-35.2)。

结论

我们得出结论,人类和病毒 DNA 在 FFPE 样本中表现出不同的衰减动力学。在评估长期储存样本中病毒 DNA 的流行率时,应考虑人类 DNA 的快速降解,因为 HPV DNA 检测仍然是病毒相关转化的关键生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7655/8008572/754793d541a7/12985_2021_1529_Fig1_HTML.jpg

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